Dynamic changes of live/apoptotic circulating tumour cells as predictive marker of response to Sunitinib in metastatic renal cancer View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2012-10

AUTHORS

E Rossi, M Fassan, M Aieta, F Zilio, R Celadin, M Borin, A Grassi, L Troiani, U Basso, C Barile, T Sava, C Lanza, L Miatello, A Jirillo, M Rugge, S Indraccolo, M Cristofanilli, A Amadori, R Zamarchi

ABSTRACT

BACKGROUND: Recently, we developed an apoptotic assay for expanding the monitoring capabilities of the circulating tumour cells (CTC) test during therapy. An automated platform for computing CTCs was integrated with a mAb (M30) targeting a neoepitope disclosed by caspase cleavage at cytokeratin 18 in early apoptosis; we showed that live CTCs were associated with progression, consistent with enhanced cell migration and invasion. The test was first applied here to mRCC. METHODS: Live/apoptotic CTCs changes were measured in mRCC patients receiving first-line Sunitinib and compared with circulating endothelial cell (CEC) levels. RESULTS: The presence of EpCAM-positive, live CTCs predicts progression in individual mRCC patient, being associated with distant metastasis under first-line Sunitinib. Synchronous detection of CTCs and CEC levels discloses for the first time an association between their dynamic changes and outcome: a rapid increase of the CEC number as early as the first cycle of therapy is associated with CTC decrease in non-progressed patients, whereas a delayed response of CECs is related to higher CTC values in the progressed group indicating treatment failure. CONCLUSION: We demonstrated that a delayed response to antiangiogenic treatment indicated by persistent detection of CECs correlates with persistent live CTCs and more aggressive disease. More... »

PAGES

1286

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/bjc.2012.388

DOI

http://dx.doi.org/10.1038/bjc.2012.388

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1051878060

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22955853


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